Canonical Allele Identifier: CA2012557580

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316994

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109318_3109319insCGTG , CM000674.2:g.3109318_3109319insCGTG	GRCh38
NC_000012.11:g.3218484_3218485insCGTG , CM000674.1:g.3218484_3218485insCGTG	GRCh37
NC_000012.10:g.3088745_3088746insCGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25599_-18+25600insCGTG MANE Select	ENSP00000011898.5:n.-18+25599_-18+25600insCGTG
ENST00000649909.1:c.-130+25599_-130+25600insCGTG	ENSP00000497370.1:n.-130+25599_-130+25600insCGTG
ENST00000011898.9:c.-18+25599_-18+25600insCGTG	ENSP00000011898.5:n.-18+25599_-18+25600insCGTG
ENST00000444315.6:c.-18+25599_-18+25600insCGTG	ENSP00000412908.2:n.-18+25599_-18+25600insCGTG
ENST00000537971.5:c.-18+31865_-18+31866insCGTG	ENSP00000444799.1:n.-18+31865_-18+31866insCGTG
NM_001168320.1:c.-18+31865_-18+31866insCGTG	NP_001161792.1:n.-18+31865_-18+31866insCGTG
NM_006675.4:c.-18+25599_-18+25600insCGTG	NP_006666.1:n.-18+25599_-18+25600insCGTG
XM_011520912.1:c.-349+25599_-349+25600insCGTG	XP_011519214.1:n.-349+25599_-349+25600insCGTG
XM_011520912.3:c.-349+25599_-349+25600insCGTG	XP_011519214.1:n.-349+25599_-349+25600insCGTG
NM_006675.5:c.-18+25599_-18+25600insCGTG MANE Select	NP_006666.1:n.-18+25599_-18+25600insCGTG
NM_001168320.2:c.-18+31865_-18+31866insCGTG	NP_001161792.1:n.-18+31865_-18+31866insCGTG